21 CFR 820 (The QSR) A practical approach to what each subpart really requires

Website http://www.onlinecompliancepanel.com/ecommerce/webinar/~product_id=500485?expDate=Ourglocal | Edit Freely

Category 13485, 21 CFR, 21 CFR 820, FDA 483, FDA warning letter, from 483, ISO 13485, medical device, QSR, quality system regulation

Deadline: September 17, 2014 | Date: September 17, 2014

Venue/Country: 38868 Salmon Ter, Fremont, U.S.A

Updated: 2014-09-16 19:15:36 (GMT+9)

Call For Papers - CFP

Description:

This webinar will focus on 21 CFR, FDA 483 and warning letter observations to understand the FDA's intent when reviewing your company's quality system.

21 CFR also called the Quality System Regulation is a 15 part regulation that looks simple enough to execute against, on paper. However, although the regulations haven't changed significantly in 30+ years, their interpretation has grown more stringent. Learn about each subpart "in a nutshell" and learn from 483 and warning letter observations to understand the FDA's intent when reviewing your company's quality system.

Why Should you Attend:

This is a very practical approach to the QSR. It teaches you about information not found in Google or forums from an instructor who has been through several FDA remediation projects for small and large companies alike.

Objectives of the Presentation:

To learn more about 21 CFR 820.

Who can Benefit:

Engineers

Quality Managers

Regulatory, managers

Quick Contact:

http://www.onlinecompliancepanel.com/ecommerce/webinar/~product_id=500485?expDate=Ourglocal

Toll free: +1-510-857-5896

Email:?webinaronlinecompliancepanel.com

OnlineCompliancePanel LLC,

38868 Salmon Ter,

Fremont, CA 94536, USA